A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063001



Internal ID19152220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27589845hg38UCSC Ensembl
Innerchr19:27747981..28080753hg19UCSC Ensembl
Innerchr19:32439821..32772593hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38332773
hg19332773
hg18332773
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3497n100
Supporting Variantsnssv3572020
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063001
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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